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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649205Generated: October 29, 2026

Carbon Disulfide → 2-(1-Imidazolyl)-2-(4-isobutyl-1,3-dithiolan-2-ylidene)acetonitrile

https://huagongshe.com/reaction/649205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
Reactant(1-Imidazolyl)acetonitrileHCID 11804695—
Reactant1,2-Dibromo-4-methylpentaneHCID 13605937—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-(1-Imidazolyl)-2-(4-isobutyl-1,3-dithiolan-2-ylidene)acetonitrileHCID 53843081—

Reaction Steps

To a mixed solution of 0.55 g (0.005 mole) of 1-cyanomethylimidazole, 0.4 g (0.005 mole) of carbon disulfide and 10 ml of dimethyl sulfoxide was added 0.8 g (0.014 mole) of potassium hydroxide powder with stirring, and the reaction was carried out at room temperature for 1 hour. Then, 1.5 g (0.006 mole) of 1,2-dibromo-4-methylpentane was added dropwise with stirring, and the resulting solution was subjected to reaction for 2 hours. After completion of the reaction, 20 ml of water was added to the reaction solution, after which the resulting mixture was subjected to extraction with ethyl acetate, and the organic layer was washed with water and dried. The solvent was distilled off and the residue was purified by silica gel chromatography to obtain 0.45 g of the Z isomer and 0.3 g of the E isomer individually in the form of colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04738976
Source datasetuspto-grants-1988_04
ORD IDord-c41aa2c9f7ca40069df0fca2f6979975
Source noteuspto-grants-1988_04